The Google Home app is getting an update with a home panel that allows users to better monitor home devices. This comes after Google announced the public rollout of the revamped version of its app.

A 15-person FDA Circulatory System Devices Panel has unanimously voted against Johnson & Johnson MedTech’s V-Wave Ventura interatrial shunt, creating a setback for the major medtech leader. The panel ...

GAITHERSBURG, MD — Instrumentation used to place surgical mesh during urogynecological procedures should be subject to stricter manufacturing requirements and more detailed labeling, according to US ...

Given the lack of information on their effectiveness and the unreasonable risks for illness or injury, spinal sphere devices should be regulated as Class 3 devices that require premarket approval (PMA ...

(Reuters) -The U.S. Food and Drug Administration's (FDA) independent experts on Wednesday narrowly voted against recommending the approval of Medtronic's blood pressure treatment device, saying risks ...